JP2007529580A5 - - Google Patents
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- Publication number
- JP2007529580A5 JP2007529580A5 JP2007503233A JP2007503233A JP2007529580A5 JP 2007529580 A5 JP2007529580 A5 JP 2007529580A5 JP 2007503233 A JP2007503233 A JP 2007503233A JP 2007503233 A JP2007503233 A JP 2007503233A JP 2007529580 A5 JP2007529580 A5 JP 2007529580A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- optionally
- compounds
- polymerization
- phenoxide
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 150000001875 compounds Chemical class 0.000 claims 12
- AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical group NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 claims 8
- 239000011230 binding agent Substances 0.000 claims 7
- 238000006116 polymerization reaction Methods 0.000 claims 6
- 238000004519 manufacturing process Methods 0.000 claims 5
- 230000005855 radiation Effects 0.000 claims 5
- PCHXZXKMYCGVFA-UHFFFAOYSA-N 1,3-diazetidine-2,4-dione Chemical group O=C1NC(=O)N1 PCHXZXKMYCGVFA-UHFFFAOYSA-N 0.000 claims 2
- 239000000654 additive Substances 0.000 claims 2
- 239000003054 catalyst Substances 0.000 claims 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims 2
- ZWRWGKGPUFESNE-UHFFFAOYSA-M 2-carboxyphenolate;tetrabutylazanium Chemical compound OC1=CC=CC=C1C([O-])=O.CCCC[N+](CCCC)(CCCC)CCCC ZWRWGKGPUFESNE-UHFFFAOYSA-M 0.000 claims 1
- JUMAVEPPATWXPU-UHFFFAOYSA-M 2-carboxyphenolate;tetrabutylphosphanium Chemical compound OC1=CC=CC=C1C([O-])=O.CCCC[P+](CCCC)(CCCC)CCCC JUMAVEPPATWXPU-UHFFFAOYSA-M 0.000 claims 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims 1
- BMPUZCYEXQPLBJ-UHFFFAOYSA-M 2-methoxycarbonylphenolate;tetrabutylazanium Chemical compound COC(=O)C1=CC=CC=C1[O-].CCCC[N+](CCCC)(CCCC)CCCC BMPUZCYEXQPLBJ-UHFFFAOYSA-M 0.000 claims 1
- AVGAKQIVSLBDJA-UHFFFAOYSA-M 2-methoxycarbonylphenolate;tetrabutylphosphanium Chemical compound COC(=O)C1=CC=CC=C1[O-].CCCC[P+](CCCC)(CCCC)CCCC AVGAKQIVSLBDJA-UHFFFAOYSA-M 0.000 claims 1
- PBFFMHHKRMHFSN-UHFFFAOYSA-M 4-formylphenolate;tetrabutylazanium Chemical compound [O-]C1=CC=C(C=O)C=C1.CCCC[N+](CCCC)(CCCC)CCCC PBFFMHHKRMHFSN-UHFFFAOYSA-M 0.000 claims 1
- NHGSIJKJYSAVEJ-UHFFFAOYSA-M 4-formylphenolate;tetrabutylphosphanium Chemical compound [O-]C1=CC=C(C=O)C=C1.CCCC[P+](CCCC)(CCCC)CCCC NHGSIJKJYSAVEJ-UHFFFAOYSA-M 0.000 claims 1
- NDWUBGAGUCISDV-UHFFFAOYSA-N 4-hydroxybutyl prop-2-enoate Chemical compound OCCCCOC(=O)C=C NDWUBGAGUCISDV-UHFFFAOYSA-N 0.000 claims 1
- UYOMRLLJHAQWMZ-UHFFFAOYSA-M 4-methoxycarbonylphenolate;tetrabutylazanium Chemical compound COC(=O)C1=CC=C([O-])C=C1.CCCC[N+](CCCC)(CCCC)CCCC UYOMRLLJHAQWMZ-UHFFFAOYSA-M 0.000 claims 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 claims 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical group OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 1
- 230000003213 activating effect Effects 0.000 claims 1
- 239000011248 coating agent Substances 0.000 claims 1
- 239000008199 coating composition Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 239000003999 initiator Substances 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 claims 1
- 125000000962 organic group Chemical group 0.000 claims 1
- 125000004430 oxygen atom Chemical group O* 0.000 claims 1
- 239000005056 polyisocyanate Substances 0.000 claims 1
- 229920001228 polyisocyanate Polymers 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical compound CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 claims 1
- BJQWBACJIAKDTJ-UHFFFAOYSA-N tetrabutylphosphanium Chemical compound CCCC[P+](CCCC)(CCCC)CCCC BJQWBACJIAKDTJ-UHFFFAOYSA-N 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102004012903A DE102004012903A1 (de) | 2004-03-17 | 2004-03-17 | Niedrigviskose Allophanate mit aktinisch härtbaren Gruppen |
| DE102004012903.7 | 2004-03-17 | ||
| PCT/EP2005/002334 WO2005092942A1 (de) | 2004-03-17 | 2005-03-05 | Niedrigviskose allophanate mit aktinisch härtbaren gruppen |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2007529580A JP2007529580A (ja) | 2007-10-25 |
| JP2007529580A5 true JP2007529580A5 (enExample) | 2008-04-24 |
| JP4995073B2 JP4995073B2 (ja) | 2012-08-08 |
Family
ID=34961838
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007503233A Expired - Fee Related JP4995073B2 (ja) | 2004-03-17 | 2005-03-05 | 化学線硬化性基を含む低粘度アロファネート |
Country Status (11)
| Country | Link |
|---|---|
| US (2) | US7361723B2 (enExample) |
| EP (1) | EP1742976B1 (enExample) |
| JP (1) | JP4995073B2 (enExample) |
| KR (1) | KR101168445B1 (enExample) |
| CN (1) | CN100516106C (enExample) |
| AT (1) | ATE481436T1 (enExample) |
| BR (1) | BRPI0508905A (enExample) |
| CA (1) | CA2559734C (enExample) |
| DE (2) | DE102004012903A1 (enExample) |
| ES (1) | ES2350696T3 (enExample) |
| WO (1) | WO2005092942A1 (enExample) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102004043342A1 (de) * | 2004-09-08 | 2006-03-09 | Bayer Materialscience Ag | Blockierte Polyurethan-Prepolymere als Klebstoffe |
| DE102004043538A1 (de) * | 2004-09-09 | 2006-03-16 | Bayer Materialscience Ag | Herstellung von neuen strahlenhärtenden Bindemitteln |
| DE102004043540A1 (de) | 2004-09-09 | 2006-03-30 | Bayer Materialscience Ag | Niedrigviskose Allophanate mit aktinisch härtbaren Gruppen |
| DE102004048775A1 (de) * | 2004-10-07 | 2006-04-13 | Degussa Ag | Hoch reaktive uretdiongruppenhaltige Polyurethanzusammensetzungen |
| DE102004048873A1 (de) | 2004-10-07 | 2006-04-13 | Bayer Materialscience Ag | Verfahren zur Herstellung von niedrigviskosen Allophanaten mit aktinisch härtbaren Gruppen |
| DE102006015709A1 (de) * | 2006-04-04 | 2007-10-11 | Bayer Materialscience Ag | Verfahren zur Herstellung von allophanathaltigen, durch aktinische Strahlung härtbaren Polyurethanprepolymeren mit erhöhter Beständigkeit |
| DE102007040239A1 (de) | 2007-08-25 | 2009-05-07 | Bayer Materialscience Ag | Verfahren zur Herstellung von niedrigviskosen Allophanaten mit aktinisch härtbaren Gruppen |
| DE102007040240A1 (de) * | 2007-08-25 | 2009-02-26 | Bayer Materialscience Ag | Verfahren zur Herstellung von niedrigviskosen Allophanaten mit aktinisch härtbaren Gruppen |
| JP5379014B2 (ja) | 2007-10-15 | 2013-12-25 | 三井化学株式会社 | 粒子状ポリウレタン樹脂組成物およびその成形品 |
| US8722752B2 (en) * | 2007-10-15 | 2014-05-13 | Mitsui Chemicals, Inc. | Polyurethane resin |
| WO2009069433A1 (ja) * | 2007-11-28 | 2009-06-04 | Mitsui Chemicals Polyurethanes, Inc. | 反応射出成形用ポリウレタン樹脂組成物および成形品 |
| US9102785B2 (en) * | 2008-04-11 | 2015-08-11 | Ppg Industries Ohio, Inc. | Curable compositions based on polyuretidiones, polythiols and photoactivable bases and generation of isocyanates from uretidiones |
| KR101048329B1 (ko) | 2008-10-06 | 2011-07-14 | 주식회사 엘지화학 | 우레탄계 다관능성 모노머, 그의 제조방법 및 이를 포함하는 감광성 수지 조성물 |
| DE102009008569A1 (de) * | 2009-02-12 | 2010-08-19 | Bayer Materialscience Ag | Verfahren zur Herstellung von besonders reaktiven und niedrigviskosen Allophanaten mit aktinisch härtbaren Gruppen und deren Verwendung zur Herstellung besonders kratzfester Beschichtungen |
| PL2581398T3 (pl) | 2011-10-14 | 2015-02-27 | Allnex Ip Sarl | Sposób wytwarzania emulgowalnych w wodzie allofanianów o małej lepkości z grupami utwardzalnymi promieniowaniem |
| EP2581397B1 (de) | 2011-10-14 | 2014-12-10 | Allnex IP S.à.r.l. | Verfahren zur herstellung von niedrigviskosen, wasserverdünnbaren urethan(meth)acrylaten |
| KR101871611B1 (ko) | 2013-10-11 | 2018-06-27 | 트랜지션즈 옵티칼 인코포레이티드 | 광학 기판에 다중 코팅을 도포하기 위한 스핀 코터 |
| MX2016016630A (es) | 2014-06-23 | 2017-06-06 | Carbon Inc | Metodos para producir objetos tridimensionales de poliuretano a partir de materiales que tienen multiples mecanismos de endurecimiento. |
| US10316213B1 (en) | 2017-05-01 | 2019-06-11 | Formlabs, Inc. | Dual-cure resins and related methods |
| CN110028404B (zh) * | 2018-01-11 | 2023-01-24 | 深圳有为技术控股集团有限公司 | 低粘度丙烯酸酯型化合物及其复配应用体系 |
| WO2019183330A1 (en) * | 2018-03-23 | 2019-09-26 | Covestro Llc | Basecoat acid neutralization through inorganic salts |
| CN115181539B (zh) * | 2022-09-08 | 2022-12-20 | 拓迪化学(上海)有限公司 | 一种用于电池的uv光固化型胶水及其应用 |
Family Cites Families (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB994890A (en) | 1961-12-18 | 1965-06-10 | Ici Ltd | New organic polyisocyanates and their manufacture |
| US4108814A (en) * | 1974-09-28 | 1978-08-22 | Bayer Aktiengesellschaft | Aqueous polyurethane dispersions from solvent-free prepolymers using sulfonate diols |
| DE2729990A1 (de) * | 1977-07-02 | 1979-01-18 | Bayer Ag | Verfahren zur herstellung von isocyanatgruppen aufweisenden allophanaten |
| US4542165A (en) * | 1983-09-08 | 1985-09-17 | Sanyo Chemical Industries, Ltd. | Polyurethane based on epoxy-containing polymer polyol and process for making the same |
| US4717738A (en) * | 1985-01-22 | 1988-01-05 | Sanyo Chemical Industries, Ltd. | Polyurethane based on hydroxyl-containing polymer polyol and process for making the same |
| JPS63145320A (ja) * | 1986-12-09 | 1988-06-17 | Sanyo Chem Ind Ltd | ポリウレタンの製法 |
| US5905151A (en) * | 1993-02-18 | 1999-05-18 | Bayer Corporation | Trimer catalyst for aliphatic and aromatic isocyanates |
| DE4416321A1 (de) * | 1994-05-09 | 1995-11-16 | Bayer Ag | Verfahren zur Herstellung von Allophanatgruppen aufweisenden lichtechten Polyisocyanaten |
| DE4441176A1 (de) * | 1994-11-18 | 1996-05-23 | Bayer Ag | Allophanatgruppen aufweisende Polyisocyanate |
| JPH08283657A (ja) * | 1995-04-12 | 1996-10-29 | Nippon Paint Co Ltd | 塗料用硬化性樹脂組成物 |
| DE19632951A1 (de) * | 1996-08-19 | 1998-02-26 | Bayer Ag | Verfahren zur Herstellung von aliphatischen und/oder cycloaliphatischen und/oder Isocyanatgruppen aufweisenden Allophanaten |
| US5739251A (en) * | 1997-03-27 | 1998-04-14 | Bayer Corporation | Low viscosity, ethylenically unsaturated polyurethanes containing allophanate groups |
| US5777024A (en) * | 1997-04-30 | 1998-07-07 | The Valspar Corporation | Urethane resins and coating compositions and methods for their use |
| US5767220A (en) * | 1997-08-25 | 1998-06-16 | Bayer Corporation | Low viscosity, ethylenically unsaturated polyurethanes containing allophanate groups |
| DE19739970A1 (de) * | 1997-09-11 | 1999-03-18 | Basf Ag | Strahlungshärtbare Zubereitungen auf der Basis aliphatischer, Urethangruppen enthaltender Prepolymere mit ethylenisch ungesättigten Doppelbindungen |
| DE19750186A1 (de) | 1997-11-13 | 1999-05-20 | Bayer Ag | Hydrophilierungsmittel, ein Verfahren zu dessen Herstellung sowie dessen Verwendung als Dispergator für wäßrige Polyurethan-Dispersionen |
| DE19853569A1 (de) * | 1998-11-20 | 2000-05-25 | Bayer Ag | Neue Urethanacrylate, Verfahren zu ihrer Herstellung sowie ihre Verwendung |
| DE19860041A1 (de) * | 1998-12-23 | 2000-06-29 | Basf Ag | Durch Addition an Isocyanatgruppen als auch durch strahlungsinduzierte Addition an aktivierte C-C-Doppelbindungen härtbare Beschichtungsmittel |
| US6472493B1 (en) * | 1999-11-23 | 2002-10-29 | E. I. Du Pont De Nemours And Company | Clear coating composition having improved early hardness and water resistance |
| US6534128B1 (en) * | 2000-11-09 | 2003-03-18 | 3M Innovative Properties Company | Inks and other compositions incorporating low viscosity, radiation curable, polyester urethane oligomer |
| FR2818974B1 (fr) * | 2000-12-29 | 2003-10-24 | Rhodia Chimie Sa | (cyclo) condensation de composes isocyanates |
| JP4678466B2 (ja) * | 2001-08-09 | 2011-04-27 | Dic株式会社 | エネルギー線硬化型樹脂組成物 |
| DE10205608A1 (de) * | 2002-02-11 | 2003-08-21 | Degussa | Bei niedriger Temperatur härtbare feste uretdiongruppenhaltige Polyurethan-Pulverlackzusammensetzungen |
| DE10346957A1 (de) * | 2003-10-09 | 2005-05-04 | Degussa | Hochreaktive, flüssige uretdiongruppenhaltige Polyurenthansysteme, die bei niedriger Temperatur härtbar sind |
| DE102004012902A1 (de) * | 2004-03-17 | 2005-10-06 | Bayer Materialscience Ag | Herstellung von neuen strahlenhärtenden Bindemitteln |
| US7135505B2 (en) * | 2004-10-25 | 2006-11-14 | Bayer Materialscience Llc | Radiation curable coatings based on uretdione polyisocyanates |
-
2004
- 2004-03-17 DE DE102004012903A patent/DE102004012903A1/de not_active Withdrawn
-
2005
- 2005-03-05 AT AT05715756T patent/ATE481436T1/de active
- 2005-03-05 CN CNB2005800086393A patent/CN100516106C/zh not_active Expired - Lifetime
- 2005-03-05 KR KR1020067019006A patent/KR101168445B1/ko not_active Expired - Fee Related
- 2005-03-05 ES ES05715756T patent/ES2350696T3/es not_active Expired - Lifetime
- 2005-03-05 BR BRPI0508905-0A patent/BRPI0508905A/pt active Search and Examination
- 2005-03-05 CA CA2559734A patent/CA2559734C/en not_active Expired - Fee Related
- 2005-03-05 WO PCT/EP2005/002334 patent/WO2005092942A1/de not_active Ceased
- 2005-03-05 EP EP05715756A patent/EP1742976B1/de not_active Expired - Lifetime
- 2005-03-05 JP JP2007503233A patent/JP4995073B2/ja not_active Expired - Fee Related
- 2005-03-05 DE DE502005010266T patent/DE502005010266D1/de not_active Expired - Lifetime
- 2005-03-14 US US11/080,706 patent/US7361723B2/en active Active
-
2008
- 2008-02-22 US US12/072,022 patent/US7960446B2/en not_active Expired - Lifetime
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